Product database and activity tracking
Our medicinal product database (RIMS) has been configured with a focus on pharmaceutical companies managing product information, activities, and related documents, in both EU and non-EU countries.
READY! RIMS
The web user interface supports collaboration among various departments or geographic locations.
READY! medicinal product database configuration is a web-based, innovative Regulatory Information Management system (RIMS) handling your organisation’s critical data in a single reference source.
Using READY! is simple and users like it.
READY! product database (RIMS) configuration provides:
- Regulatory database storing information about human and veterinary medicinal products, APIs and medical devices
- Support for EU and non-EU regulatory procedures
- Tracking of activities
- Tracking of important dates and deadlines
- Automatic monitoring of deadlines and sending alerts via email
- Document workflow and approval
- Archiving important documents (MAs, commitments, SmPCs, PILs, etc.)
- Archiving submissions in various formats, including eCTD and NeeS
- Article 57 submissions
- Organisations management:
– Manufactures (APIs, finished, intermediates, packaging, batch releasers)
– Partners (co-development, in-licensing, out-licensing, etc.)
– Distributors - Packaging info & storage conditions
- Additional custom data
READY! is based on ISO IDMP standards and SPOR controlled vocabularies. It can be easily configured to meet your specific company requirements.
With our regulatory database configuration your can efficiently plan, track, and monitor all activities and tasks in various departments. Automatic reminders and email alerts help users focus on their daily work and never miss deadlines.
READY! is a replacement for all those Excel spreadsheets that you are using across your company.
READY! SOLUTIONS
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READY! for ePI
Prepare, submit, and maintain documents in ePI with our pre-configured READY! platform.
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Product information, Labelling
Increase efficiency in the approval of PI during regulatory procedures.
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Regulatory Affairs
Replace Excel spreadsheets, shared drives, and outdated regulatory databases.
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Article 57 reporting gateway
Exchange medicinal product information with a click on one button.
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Pharmacovigilance
Promote, maintain, and improve compliance with the legal requirements.
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Development
Track milestones and store documents created in the development of a new medicine.
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Quality Assurance
Manage processes, documents, and products in one integrated platform.
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Are you READY! ?
Manage product information, safety data, and documents in one validated environment.
READY!® stands for: REgulated Affairs DiarY
READY! is based around the idea that companies need updated, current information about their products in all of their iterations.
READY! has been developed to meet specific needs of management of structured (IDMP medicinal product information) and unstructured information (documents, forms, records) in pharma industry.
